Clinical Research Coordinator

Mass General Brigham•Boston, MA

1d•$21 - $29•Onsite

About The Position

Mass General Brigham is seeking a motivated individual for a Clinical Research Coordinator position in the MGH Food Allergy Center (FAC). The FAC is a multidisciplinary research center focused on investigating new therapeutic modalities for food allergies and understanding the mechanisms of allergic disease. The incidence of food allergy is rising, and current treatments are limited. The FAC is committed to exploring underlying pathways and potential therapies through multiple clinical trials. This position's primary focus is coordinating these clinical trials, involving protocol management, patient screening, data collection, ensuring compliance, reporting adverse events, monitoring treatment, managing laboratory samples, and maintaining research files. This role is ideal for individuals interested in gaining significant experience in medical research and considering future medical or graduate studies. The successful candidate will be encouraged and supported in seeking educational opportunities and academic productivity. The position requires a Bachelor's Degree in a related field, with experience in research project work preferred (0-1 year). Candidates in the process of completing their bachelor's degree have a six-month grace period (up to one year if starting per diem) to provide degree equivalency verification. This role does not require direct patient care.

Requirements

Bachelor's Degree Related Field of Study required
Some relevant research project work 0-1 year preferred
Careful attention to detail and good organizational skills.
Ability to follow directions.
Good interpersonal and communication skills.
Computer literacy.
Working knowledge of clinical research protocols.
Ability to demonstrate respect and professionalism for subjects' rights and individual needs.

Nice To Haves

Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification.

Responsibilities

Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
Recruiting patients for clinical trials and conducting phone interviews.
Verifies the accuracy of study forms and updates them per protocol.
Prepares data for analysis and data entry.
Documents patient visits and procedures.
Assists with regulatory binders and QA/QC Procedures.
Assists with interviewing study subjects.
Assists with study regulator submissions.
Screening for patient eligibility.
Data collection.
Ensuring protocol compliance.
Adverse drug reaction reports.
Monitoring subject treatment.
Laboratory and specimen submission.
Maintenance of accurate and complete clinical research files.
Collecting and organizing patient data.
Scheduling patients for study visits.
Performing clinical tests such as phlebotomy, EKGs, etc.
Maintaining and updating data generated by the study.